Variant report

Variant rs1867849
Chromosome Location chr2:63726932-63726933
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:20 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:63688600-63727800 Weak transcription Primary B cells from cord blood blood
2 chr2:63690600-63733000 Weak transcription Dnd41 blood
3 chr2:63691400-63728000 Weak transcription Primary hematopoietic stem cells blood
4 chr2:63698600-63733600 Weak transcription Primary T cells from cord blood blood
5 chr2:63712200-63727600 Weak transcription Fetal Heart heart
6 chr2:63715600-63727000 Weak transcription Pancreas Pancrea
7 chr2:63716800-63733400 Weak transcription Primary hematopoietic stem cells short term culture blood
8 chr2:63718000-63729600 Weak transcription Aorta Aorta
9 chr2:63724600-63735200 Weak transcription H9 Cell Line embryonic stem cell
10 chr2:63725200-63727000 Weak transcription NHEK skin
11 chr2:63725200-63727200 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
12 chr2:63725800-63727200 Weak transcription iPS-18 Cell Line embryonic stem cell
13 chr2:63726000-63727200 Weak transcription HUES48 Cell Line embryonic stem cell
14 chr2:63726000-63727400 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
15 chr2:63726200-63731600 Weak transcription iPS-20b Cell Line embryonic stem cell
16 chr2:63726600-63727000 Enhancers Breast Myoepithelial Primary Cells Breast
17 chr2:63726800-63727000 Genic enhancers Left Ventricle heart
18 chr2:63726800-63727000 Enhancers Psoas Muscle Psoas
19 chr2:63726800-63727200 Enhancers Esophagus oesophagus
20 chr2:63726800-63727200 Enhancers Gastric stomach

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